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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382154Generated: October 29, 2026

4'-bromo-[1,1'-Biphenyl]-4-carbonitrile → 4'-Furan-3-yl-biphenyl-4-carbonitrile

https://huagongshe.com/reaction/382154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-bromo-[1,1'-Biphenyl]-4-carbonitrileHCID 1394462—
Reactant3-(Biphenyl-4-yl)furanHCID 18380293—
SolventMethanolHCID 887—
Product4'-Furan-3-yl-biphenyl-4-carbonitrileHCID 1838041753%

Reaction Steps

As described in Example 1(a) for the preparation of 3-biphenyl-4-yl-furan, crude 4′-bromo-biphenyl-4-carbonitrile (200 mg, 0.775 mmol) and 3-fuiranboronic acid (see Thompson, W. J.; Gaudino, G. J. Org. Chem. 1984, 49, 5237-5243; 105 mg, 0.937 mmol) in MeOH (2 mL) were coupled to give a yellow solid, which was purified via preparative TLC. Elution with EtOAc:benzene (1:99) provided 100 mg (53%) of 4′-furan-3-yl-biphenyl-4-carbonitrile as a grey powder, mp 199-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306892B1
Source datasetuspto-grants-2001_10
ORD IDord-d45b95a734d74dbea0a576924887c31a
Source noteuspto-grants-2001_10